Notice
- Important: This guidance is under active development by NHS England and content may be added or updated on a regular basis.
- This Implementation Guide is currently in Draft and SHOULD NOT be used for development or active implementation without express direction from the NHS England Genomics Unit.
ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example
Example of a ServiceRequest which has been modified. After modification, the ServiceRequest SHALL include a meta.lastUpdated element and a relevantHitory element referencing the provenance resource detailing the change.
ServiceRequest |
id : ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example |
meta |
versionId : 2 |
lastUpdated : 2023-08-08T15:43:00Z |
extension |
url : https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage |
value |
coding |
system : https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory |
code : nhs-england |
display : NHS England |
status : revoked |
intent : order |
category |
coding |
system : https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory |
code : rare-disease-non-wgs |
display : Rare Disease - Non-WGS |
priority : routine |
code |
coding |
system : https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory |
code : R67.1 |
display : Monogenic hearing loss |
version : 7 |
subject |
reference : Patient/Patient-MeirLieberman-Example |
identifier |
system : https://fhir.nhs.uk/Id/nhs-number |
value : 9449307873 |
authoredOn : 2023-08-08T15:43:00Z |
requester |
reference : PractitionerRole/PractitionerRole-GeneSmithENT-Example |
reasonCode |
coding |
system : https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics |
code : diagnostic |
display : Diagnostic |
supportingInfo |
reference : Observation/Observation-GenomicEthnicity-Example |
supportingInfo |
reference : Observation/Observation-NoPregnancy-Example |
supportingInfo |
reference : Observation/Observation-DiseaseStatus-Example |
supportingInfo |
reference : Observation/Observation-NonConsanguinousUnion-Example |
supportingInfo |
reference : Observation/Observation-NoBoneMarrowTransplant-Example |
supportingInfo |
reference : Observation/Observation-NoTransfusion-Example |
supportingInfo |
reference : Observation/Observation-RiskOfInfection-Example |
supportingInfo |
reference : Observation/Observation-NatureAndAgeOfHearingLoss-Example |
specimen |
display : Specimen/Specimen-BloodEDTA-Example |
note |
text : Test no longer required. |
note |
text : Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms Patient in need of test...example |
{ "resourceType": "ServiceRequest", "id": "ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example", "meta": { "versionId": "2", "lastUpdated": "2023-08-08T15:43:00Z" }, "extension": [ { "url": "https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage", "valueCodeableConcept": { "coding": [ { "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory", "code": "nhs-england", "display": "NHS England" } ] } } ], "status": "revoked", "intent": "order", "category": [ { "coding": [ { "system": "https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory", "code": "rare-disease-non-wgs", "display": "Rare Disease - Non-WGS" } ] } ], "priority": "routine", "code": { "coding": [ { "system": "https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory", "code": "R67.1", "display": "Monogenic hearing loss", "version": "7" } ] }, "subject": { "reference": "Patient/Patient-MeirLieberman-Example", "identifier": { "system": "https://fhir.nhs.uk/Id/nhs-number", "value": "9449307873" } }, "authoredOn": "2023-08-08T15:43:00Z", "requester": { "reference": "PractitionerRole/PractitionerRole-GeneSmithENT-Example" }, "reasonCode": [ { "coding": [ { "system": "https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics", "code": "diagnostic", "display": "Diagnostic" } ] } ], "supportingInfo": [ { "reference": "Observation/Observation-GenomicEthnicity-Example" }, { "reference": "Observation/Observation-NoPregnancy-Example" }, { "reference": "Observation/Observation-DiseaseStatus-Example" }, { "reference": "Observation/Observation-NonConsanguinousUnion-Example" }, { "reference": "Observation/Observation-NoBoneMarrowTransplant-Example" }, { "reference": "Observation/Observation-NoTransfusion-Example" }, { "reference": "Observation/Observation-RiskOfInfection-Example" }, { "reference": "Observation/Observation-NatureAndAgeOfHearingLoss-Example" } ], "specimen": [ { "display": "Specimen/Specimen-BloodEDTA-Example" } ], "note": [ { "text": "Test no longer required." }, { "text": "Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms Patient in need of test...example" } ] }
<ServiceRequest xmlns="http://hl7.org/fhir"> <id value="ServiceRequest-NonWGSTestOrderFormUpdated-Cancellation-Example" /> <meta> <versionId value="2" /> <lastUpdated value="2023-08-08T15:43:00Z" /> </meta> <extension url="https://fhir.hl7.org.uk/StructureDefinition/Extension-UKCore-Coverage"> <valueCodeableConcept> <coding> <system value="https://fhir.hl7.org.uk/CodeSystem/UKCore-FundingCategory" /> <code value="nhs-england" /> <display value="NHS England" /> </coding> </valueCodeableConcept> </extension> <status value="revoked" /> <intent value="order" /> <category> <coding> <system value="https://fhir.hl7.org.uk/CodeSystem/UKCore-GenomeSequencingCategory" /> <code value="rare-disease-non-wgs" /> <display value="Rare Disease - Non-WGS" /> </coding> </category> <priority value="routine" /> <code> <coding> <system value="https://fhir.nhs.uk/CodeSystem/England-GenomicTestDirectory" /> <version value="7" /> <code value="R67.1" /> <display value="Monogenic hearing loss" /> </coding> </code> <subject> <reference value="Patient/Patient-MeirLieberman-Example" /> <identifier> <system value="https://fhir.nhs.uk/Id/nhs-number" /> <value value="9449307873" /> </identifier> </subject> <authoredOn value="2023-08-08T15:43:00Z" /> <requester> <reference value="PractitionerRole/PractitionerRole-GeneSmithENT-Example" /> </requester> <reasonCode> <coding> <system value="https://fhir.nhs.uk/CodeSystem/reasonfortesting-genomics" /> <code value="diagnostic" /> <display value="Diagnostic" /> </coding> </reasonCode> <supportingInfo> <reference value="Observation/Observation-GenomicEthnicity-Example" /> </supportingInfo> <supportingInfo> <reference value="Observation/Observation-NoPregnancy-Example" /> </supportingInfo> <supportingInfo> <reference value="Observation/Observation-DiseaseStatus-Example" /> </supportingInfo> <supportingInfo> <reference value="Observation/Observation-NonConsanguinousUnion-Example" /> </supportingInfo> <supportingInfo> <reference value="Observation/Observation-NoBoneMarrowTransplant-Example" /> </supportingInfo> <supportingInfo> <reference value="Observation/Observation-NoTransfusion-Example" /> </supportingInfo> <supportingInfo> <reference value="Observation/Observation-RiskOfInfection-Example" /> </supportingInfo> <supportingInfo> <reference value="Observation/Observation-NatureAndAgeOfHearingLoss-Example" /> </supportingInfo> <specimen> <display value="Specimen/Specimen-BloodEDTA-Example" /> </specimen> <note> <text value="Test no longer required." /> </note> <note> <text value="Free text for diagnosis/reason for referral, relevant information including family history, phenotypic details/ HPO Terms Patient in need of test...example" /> </note> </ServiceRequest>